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首页> 外文期刊>Cellulose Chemistry and Technology: International Journal for Physics, Chemistry and Technology of Cellulose and Lignin >OPTIMIZATION OF SUBMERGED FERMENTATION CONDITIONS FOR TWO XYLANASE PRODUCERS COPRINELLUS DISSEMINATUS MLK-01NTCC-1180 AND MLK-07NTCC-1181 AND THEIR BIOCHEMICAL CHARACTERIZATION
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OPTIMIZATION OF SUBMERGED FERMENTATION CONDITIONS FOR TWO XYLANASE PRODUCERS COPRINELLUS DISSEMINATUS MLK-01NTCC-1180 AND MLK-07NTCC-1181 AND THEIR BIOCHEMICAL CHARACTERIZATION

机译:两种木聚糖酶生产假单胞菌MLK-01NTCC-1180和MLK-07NTCC-1181的深层发酵条件的优化及其生化特性

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摘要

Out of 15 isolates, two white-rot basidiomycetes, namely MLK-01 and MLK-07, showed good growth in the pH range of 5.0 to 10.0. Both isolates produced maximal fungal growth and xylanase activity with minimal cellulase contamination at incubation periods of 8 and 9 days, respectively, and pH 10.0 with wheat bran as substrate under submerged fermentation conditions. The maximum xylanase, CMCase and lignin peroxidase activities of isolate MLK-01 were 30.32, 0.32 and 0.25 IU/mL, respectively, with protein concentration of 1.76 mg/mL at pH 7.5 and temperature of 75 degrees C, while those of isolate MLK-07 were 36.37, 0.25 and 0.15 IU/mL with protein concentration of 1.69 at pH 8.0 and temperature of 65 degrees C. Hg2+ and Cu2+ inhibited the xylanase activity for isolate MLK-01 to 17.6 and 20.20%, and for MLK-07 to 82.2 and 70.5%, respectively. All the metallic ions like Ca2+, Mn2+, Fe2+, Pb2+, Mg2+, Ni2+, K+, Na+ and Zn2+ improved the enzyme activity, but the enzyme activity doubled with Zn2+ for isolate MLK-01 and with Fe2+ for isolate MLK-07.
机译:在15种分离物中,两种白腐担子菌,即MLK-01和MLK-07,在5.0至10.0的pH范围内均表现出良好的生长。两种分离物分别在淹没发酵条件下分别在8天和9天的温育期和以麦麸为底物的pH 10.0时产生了最大的真菌生长和木聚糖酶活性,同时纤维素酶的污染也最小。分离株MLK-01的最大木聚糖酶,CMCase和木质素过氧化物酶活性分别为30.32、0.32和0.25 IU / mL,在pH 7.5和温度为75摄氏度时蛋白浓度为1.76 mg / mL,而分离株MLK- 07分别为36.37、0.25和0.15 IU / mL,在pH 8.0和65摄氏度的温度下蛋白浓度为1.69。Hg2+和Cu2 +抑制分离株MLK-01的木聚糖酶活性至17.6和20.20%,而MLK-07的木聚糖酶活性至82.2。和70.5%。诸如Ca2 +,Mn2 +,Fe2 +,Pb2 +,Mg2 +,Ni2 +,K +,Na +和Zn2 +的所有金属离子均提高了酶的活性,但是对于MLK-01分离物和MLK-07分离物,Fe2 +的酶活性增加了一倍。

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